US5130036A - Phosphorous amine lubricant additives - Google Patents
Phosphorous amine lubricant additives Download PDFInfo
- Publication number
- US5130036A US5130036A US07/526,080 US52608090A US5130036A US 5130036 A US5130036 A US 5130036A US 52608090 A US52608090 A US 52608090A US 5130036 A US5130036 A US 5130036A
- Authority
- US
- United States
- Prior art keywords
- reaction
- product
- additives
- phosphorous acid
- amine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000003879 lubricant additive Substances 0.000 title claims abstract description 11
- -1 Phosphorous amine Chemical class 0.000 title claims description 13
- 239000000203 mixture Substances 0.000 claims abstract description 44
- 150000001412 amines Chemical class 0.000 claims abstract description 42
- 239000003921 oil Substances 0.000 claims abstract description 32
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims abstract description 26
- 238000005555 metalworking Methods 0.000 claims abstract description 25
- 239000000047 product Substances 0.000 claims description 29
- 238000006243 chemical reaction Methods 0.000 claims description 28
- 239000007795 chemical reaction product Substances 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 239000000314 lubricant Substances 0.000 claims description 13
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 10
- 239000010687 lubricating oil Substances 0.000 claims description 9
- 230000001050 lubricating effect Effects 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 150000002431 hydrogen Chemical group 0.000 claims 1
- 239000000654 additive Substances 0.000 abstract description 41
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 12
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 abstract description 12
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract description 7
- 239000012188 paraffin wax Substances 0.000 abstract description 3
- 239000005069 Extreme pressure additive Substances 0.000 abstract description 2
- 238000005580 one pot reaction Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 description 25
- 150000001639 boron compounds Chemical class 0.000 description 20
- 230000000996 additive effect Effects 0.000 description 17
- 239000011541 reaction mixture Substances 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000012530 fluid Substances 0.000 description 10
- 239000007788 liquid Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 8
- 239000004327 boric acid Substances 0.000 description 8
- 239000010699 lard oil Substances 0.000 description 8
- 239000002480 mineral oil Substances 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 6
- 229910052796 boron Inorganic materials 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 5
- 239000010931 gold Substances 0.000 description 5
- 229910052737 gold Inorganic materials 0.000 description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
- 230000035484 reaction time Effects 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000012263 liquid product Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- 229910001018 Cast iron Inorganic materials 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical class O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 238000003754 machining Methods 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 231100000241 scar Toxicity 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 2
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- AAIUWVOMXTVLRG-UHFFFAOYSA-N 8,8-dimethylnonan-1-amine Chemical compound CC(C)(C)CCCCCCCN AAIUWVOMXTVLRG-UHFFFAOYSA-N 0.000 description 2
- 229910011255 B2O3 Inorganic materials 0.000 description 2
- 229910001369 Brass Inorganic materials 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical class O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 2
- 239000011369 resultant mixture Substances 0.000 description 2
- 238000010079 rubber tapping Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 238000007039 two-step reaction Methods 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- ZBUAAIKWLHWSPO-UHFFFAOYSA-N (Z)-20-aminoicos-11-en-1-ol Chemical compound OCCCCCCCCCCC=C/CCCCCCCCN ZBUAAIKWLHWSPO-UHFFFAOYSA-N 0.000 description 1
- OXUBFNFJCLTHCF-UHFFFAOYSA-N 1-(hexylamino)propan-2-ol Chemical compound CCCCCCNCC(C)O OXUBFNFJCLTHCF-UHFFFAOYSA-N 0.000 description 1
- KQGQJTIIVFAWCS-UHFFFAOYSA-N 1-(icosylamino)propan-2-ol Chemical compound CCCCCCCCCCCCCCCCCCCCNCC(C)O KQGQJTIIVFAWCS-UHFFFAOYSA-N 0.000 description 1
- FZDIQIDGTGANGI-UHFFFAOYSA-N 1-(octylamino)propan-2-ol Chemical compound CCCCCCCCNCC(C)O FZDIQIDGTGANGI-UHFFFAOYSA-N 0.000 description 1
- FNOYIJREXTXXSA-UHFFFAOYSA-N 1-(pentadecylamino)propan-2-ol Chemical compound CCCCCCCCCCCCCCCNCC(C)O FNOYIJREXTXXSA-UHFFFAOYSA-N 0.000 description 1
- OTBNHPAEPOLSAB-UHFFFAOYSA-N 1-(tetradecylamino)propan-2-ol Chemical compound CCCCCCCCCCCCCCNCC(C)O OTBNHPAEPOLSAB-UHFFFAOYSA-N 0.000 description 1
- MGJUFMASSXOBFW-UHFFFAOYSA-N 1-(triacontylamino)propan-2-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCNCC(C)O MGJUFMASSXOBFW-UHFFFAOYSA-N 0.000 description 1
- GSLZVMNQWHKUMU-UHFFFAOYSA-N 1-[2-hydroxypropyl(icosyl)amino]propan-2-ol Chemical compound CCCCCCCCCCCCCCCCCCCCN(CC(C)O)CC(C)O GSLZVMNQWHKUMU-UHFFFAOYSA-N 0.000 description 1
- QNRXIVCOPVCHAA-UHFFFAOYSA-N 1-[2-hydroxypropyl(octyl)amino]propan-2-ol Chemical compound CCCCCCCCN(CC(C)O)CC(C)O QNRXIVCOPVCHAA-UHFFFAOYSA-N 0.000 description 1
- SVXONRZSDVBEIK-UHFFFAOYSA-N 1-[2-hydroxypropyl(pentadecyl)amino]propan-2-ol Chemical compound CCCCCCCCCCCCCCCN(CC(C)O)CC(C)O SVXONRZSDVBEIK-UHFFFAOYSA-N 0.000 description 1
- NMEWVFFBYQFTLK-UHFFFAOYSA-N 1-[2-hydroxypropyl(tetradecyl)amino]propan-2-ol Chemical compound CCCCCCCCCCCCCCN(CC(C)O)CC(C)O NMEWVFFBYQFTLK-UHFFFAOYSA-N 0.000 description 1
- OPSGKMHXLFKLDV-UHFFFAOYSA-N 1-[2-hydroxypropyl(triacontyl)amino]propan-2-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCN(CC(C)O)CC(C)O OPSGKMHXLFKLDV-UHFFFAOYSA-N 0.000 description 1
- BZJZJFAPSOEUFE-UHFFFAOYSA-N 1-[dodecyl(2-hydroxypropyl)amino]propan-2-ol Chemical compound CCCCCCCCCCCCN(CC(C)O)CC(C)O BZJZJFAPSOEUFE-UHFFFAOYSA-N 0.000 description 1
- CFGWPTDWIBCXMS-UHFFFAOYSA-N 1-[hexyl(2-hydroxypropyl)amino]propan-2-ol Chemical compound CCCCCCN(CC(C)O)CC(C)O CFGWPTDWIBCXMS-UHFFFAOYSA-N 0.000 description 1
- AJPMQQSNPDNRBL-UHFFFAOYSA-N 1-dodecyl-7-thiabicyclo[4.1.0]hepta-2,4-dien-6-ol Chemical compound C1=CC=CC2(CCCCCCCCCCCC)C1(O)S2 AJPMQQSNPDNRBL-UHFFFAOYSA-N 0.000 description 1
- HCYSJBICYOIBLS-UHFFFAOYSA-N 2-(dodecylamino)ethanol Chemical compound CCCCCCCCCCCCNCCO HCYSJBICYOIBLS-UHFFFAOYSA-N 0.000 description 1
- MCIKGVLBLIZYRY-UHFFFAOYSA-N 2-(hexylamino)ethanol Chemical compound CCCCCCNCCO MCIKGVLBLIZYRY-UHFFFAOYSA-N 0.000 description 1
- SLXBNXFAEASNHX-UHFFFAOYSA-N 2-(icosylamino)ethanol Chemical compound CCCCCCCCCCCCCCCCCCCCNCCO SLXBNXFAEASNHX-UHFFFAOYSA-N 0.000 description 1
- UVYBWDBLVDZIOX-UHFFFAOYSA-N 2-(octylamino)ethanol Chemical compound CCCCCCCCNCCO UVYBWDBLVDZIOX-UHFFFAOYSA-N 0.000 description 1
- QJXHPFHKGPEMAM-UHFFFAOYSA-N 2-(pentadecylamino)ethanol Chemical compound CCCCCCCCCCCCCCCNCCO QJXHPFHKGPEMAM-UHFFFAOYSA-N 0.000 description 1
- OLPABIGAXAWMIZ-UHFFFAOYSA-N 2-(triacontylamino)ethanol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCNCCO OLPABIGAXAWMIZ-UHFFFAOYSA-N 0.000 description 1
- GOZCAZWSEYCAPZ-UHFFFAOYSA-N 2-[2-(hexylamino)ethoxy]ethanol Chemical compound CCCCCCNCCOCCO GOZCAZWSEYCAPZ-UHFFFAOYSA-N 0.000 description 1
- FCEWRLVEPKVKBU-UHFFFAOYSA-N 2-[2-(tert-butylamino)-1-hydroxyethyl]phenol Chemical compound CC(C)(C)NCC(O)C1=CC=CC=C1O FCEWRLVEPKVKBU-UHFFFAOYSA-N 0.000 description 1
- PNFAUXBTLQQKRI-UHFFFAOYSA-N 2-[2-hydroxyethyl(icosyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCCCCCCCN(CCO)CCO PNFAUXBTLQQKRI-UHFFFAOYSA-N 0.000 description 1
- QZQNMMLYACBCMJ-UHFFFAOYSA-N 2-[2-hydroxyethyl(octyl)amino]ethanol Chemical compound CCCCCCCCN(CCO)CCO QZQNMMLYACBCMJ-UHFFFAOYSA-N 0.000 description 1
- MOVFFQCDGPWQOJ-UHFFFAOYSA-N 2-[2-hydroxyethyl(pentadecyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCCN(CCO)CCO MOVFFQCDGPWQOJ-UHFFFAOYSA-N 0.000 description 1
- CPHJEACXPATRSU-UHFFFAOYSA-N 2-[2-hydroxyethyl(tetradecyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCN(CCO)CCO CPHJEACXPATRSU-UHFFFAOYSA-N 0.000 description 1
- GNKSKVKNFPXMRH-UHFFFAOYSA-N 2-[2-hydroxyethyl(triacontyl)amino]ethanol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCN(CCO)CCO GNKSKVKNFPXMRH-UHFFFAOYSA-N 0.000 description 1
- BITAPBDLHJQAID-KTKRTIGZSA-N 2-[2-hydroxyethyl-[(z)-octadec-9-enyl]amino]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCN(CCO)CCO BITAPBDLHJQAID-KTKRTIGZSA-N 0.000 description 1
- NKFNBVMJTSYZDV-UHFFFAOYSA-N 2-[dodecyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCCCCCCCCCN(CCO)CCO NKFNBVMJTSYZDV-UHFFFAOYSA-N 0.000 description 1
- GIACMWUKBLHAAG-UHFFFAOYSA-N 2-[hexyl(2-hydroxyethyl)amino]ethanol Chemical compound CCCCCCN(CCO)CCO GIACMWUKBLHAAG-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- LELNKZDJAWHHBE-ARJAWSKDSA-N 4-[(z)-17-aminoheptadec-8-enyl]heptane-2,6-diol Chemical compound CC(O)CC(CC(C)O)CCCCCCC\C=C/CCCCCCCCN LELNKZDJAWHHBE-ARJAWSKDSA-N 0.000 description 1
- 206010007269 Carcinogenicity Diseases 0.000 description 1
- 208000032544 Cicatrix Diseases 0.000 description 1
- YDGMGEXADBMOMJ-LURJTMIESA-N N(g)-dimethylarginine Chemical compound CN(C)C(\N)=N\CCC[C@H](N)C(O)=O YDGMGEXADBMOMJ-LURJTMIESA-N 0.000 description 1
- ZUEIVCHBEQAIAL-UHFFFAOYSA-N N-{2-hydroxyethyl}tetradecan-1-amine Chemical compound CCCCCCCCCCCCCCNCCO ZUEIVCHBEQAIAL-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- UAKRGPWZBSZRGW-UHFFFAOYSA-N OC(CCCCCCCCCC=C/CCCCCCCCN)C Chemical compound OC(CCCCCCCCCC=C/CCCCCCCCN)C UAKRGPWZBSZRGW-UHFFFAOYSA-N 0.000 description 1
- 101150108015 STR6 gene Proteins 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000007866 anti-wear additive Substances 0.000 description 1
- YDGMGEXADBMOMJ-UHFFFAOYSA-N asymmetrical dimethylarginine Natural products CN(C)C(N)=NCCCC(N)C(O)=O YDGMGEXADBMOMJ-UHFFFAOYSA-N 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- BUOSLGZEBFSUDD-BGPZCGNYSA-N bis[(1s,3s,4r,5r)-4-methoxycarbonyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 2,4-diphenylcyclobutane-1,3-dicarboxylate Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1C(C=2C=CC=CC=2)C(C(=O)O[C@@H]2[C@@H]([C@H]3CC[C@H](N3C)C2)C(=O)OC)C1C1=CC=CC=C1 BUOSLGZEBFSUDD-BGPZCGNYSA-N 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 231100000260 carcinogenicity Toxicity 0.000 description 1
- 230000007670 carcinogenicity Effects 0.000 description 1
- 229940117583 cocamine Drugs 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000004320 controlled atmosphere Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N dihydromaleimide Natural products O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical group 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000002816 fuel additive Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 239000012208 gear oil Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- YWWNNLPSZSEZNZ-UHFFFAOYSA-N n,n-dimethyldecan-1-amine Chemical compound CCCCCCCCCCN(C)C YWWNNLPSZSEZNZ-UHFFFAOYSA-N 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 238000010915 one-step procedure Methods 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229920000768 polyamine Chemical class 0.000 description 1
- 229920000728 polyester Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000037387 scars Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000010689 synthetic lubricating oil Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- LGQXXHMEBUOXRP-UHFFFAOYSA-N tributyl borate Chemical class CCCCOB(OCCCC)OCCCC LGQXXHMEBUOXRP-UHFFFAOYSA-N 0.000 description 1
- KDQYHGMMZKMQAA-UHFFFAOYSA-N trihexyl borate Chemical class CCCCCCOB(OCCCCCC)OCCCCCC KDQYHGMMZKMQAA-UHFFFAOYSA-N 0.000 description 1
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical class COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 1
- LTEHWCSSIHAVOQ-UHFFFAOYSA-N tripropyl borate Chemical class CCCOB(OCCC)OCCC LTEHWCSSIHAVOQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/251—Alcohol-fuelled engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
- C10N2040/28—Rotary engines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/30—Refrigerators lubricants or compressors lubricants
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/32—Wires, ropes or cables lubricants
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/34—Lubricating-sealants
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/36—Release agents or mold release agents
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/38—Conveyors or chain belts
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/40—Generators or electric motors in oil or gas winning field
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/42—Flashing oils or marking oils
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/44—Super vacuum or supercritical use
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/50—Medical uses
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
Definitions
- the present invention relates to reaction products of alkoxylated amines and phosphorous acid useful as lubricant additives. More particularly, the invention is directed to lubricant additives which can replace conventional chlorinated paraffins in applications such as extreme pressure metalworking.
- Chlorinated paraffin waxes particularly higher molecular weight solid or liquid chlorinated paraffins in the C 10 to C 30 range have been widely used for over fifty years in metalworking uses, particularly as lubricant additives in drawing oils, extrusion oils and soluble oils, and particularly for extreme pressure applications.
- the largest volume is in drawing oils where chlorinated waxes are used almost exclusively, mainly in mineral oils.
- the additives usually include phosphorous and sulfur compounds due to the severity of operations.
- soluble oils the chlorinated waxes are usually used in combination with fats or lard oils.
- chlorinated olefins and polyesters While many in the metalworking industry have switched to chlorinated olefins and polyesters, there is a concern among some that these chlorinated products as well may have carcinogenic properties. Hence, non-chlorinated substitutes are considered desirable. While sulfonated products have been satisfactory for light machining applications, they have not been generally satisfactory for heavier machining, such as the severe metal cuts and draws for which the chlorinated paraffins have been favored.
- non-chlorine containing additives have been developed to provide lubricating oil compositions with enhanced friction characteristics for use in engine and machinery lubricating oils and fuels.
- Such additives have included phosphorous compounds such as metal phosphonates, alkali metal salts of alkylphosphonic acids, and dihydrocarbyl hydrocarbylphosphonates; amines, such as alkoxylated amines; and certain boron-containing compounds. Examples of these prior art lubricating oil additives are discussed, for example, at column 1 of U.S. Pat. No. 4,529,528.
- Borated alkoxylated amines as thickeners for water based functional fluids. Borated alkoxylated amines are also disclosed in U.S. Pat. Nos. 4,400,284; 4,427,560; 4,490,265; 4,533,480 and 4,557,843 of Union Oil Company as intermediates for extreme pressure, anti-wear additives in lubricating compositions.
- compositions are disclosed in U.S. Pat. No. 3,553,131 of Hepplewhite, et al., in which C 6 -C 40 diaryl phosphonates (phosphites) are reacted with primary, secondary, or tertiary organic amines to produce products or mixtures which are incorporated in ester lubricants which are alleged to have higher load-carrying properties, surprising stability under storage and are relatively non-corrosive to metals.
- C 6 -C 40 diaryl phosphonates phosphites
- U.S. Pat. No. 4,857,214 also discloses phosphorous-containing compounds useful as additives in lubricants.
- the compounds of this reference comprise the oil soluble reaction product of an inorganic phosphorous acid or anhydride, a boron compound and an ashless dispersant.
- the preferred acid is phosphorous acid.
- the ashless dispersant may be, e.g., a hydrocarbyl succinimide, a mixed ester/amide of hydrocarbyl-substituted succinic acid, hydroxyesters of hydrocarbyl-substituted succinic acid, and the Mannich condensation products of hydrocarbyl-substituted phenols, formaldehyde and polyamines.
- N-tallow diethanolamine may also be used in combination with the ashless dispersant.
- N-tallow diethanolamine may also be used in combination with the ashless dispersant.
- reaction product of an alkoxylated amine and phosphorous acid may be used as a metalworking lubricant additive.
- a lubricant additive which is the reaction product of phosphorous acid with an alkoxylated amine of the formula ##STR1## wherein R is a C 6 to C 30 hydrocarbon group or an alkoxylated C 6 to C 30 hydrocarbon group, R' is a C 1 to C 6 alkylene group and R" is individually hydrogen or a C 1 to C 6 hydrocarbon group, w is 0 or and x, y and z are each integers of from 0 to 10, at least one of which is not 0, preferably about 1 to 3, and more preferably each is 1.
- a boron compound selected from boric oxide, a metaborate or a compound of the formula
- R 3 is a C 1 to C 6 alkyl group, and m and n are 0 to 3, their sum being 3, is included in the reaction with the alkoxylated amine and phosphorus acid to form the reaction product.
- R 4 and R 5 may each be a C 1 to C 30 hydrocarbon group, may be included in the reaction of the alkoxylated amine and phosphorous acid or the alkoxylated amine, phosphorous acid and boron compound to form a reaction product.
- the present invention also includes lubricating oil compositions, particularly metal-working oils, containing the above-discussed reaction products as additives.
- These lubricating compositions may include as the major component mineral oils or synthetic oils including so-called "soluble oils” for use in forming aqueous emulsion lubricants.
- the invention also includes the use of the lubricant additives in metalworking operations, particularly extreme pressure operations.
- the compounds or complexes of the present invention are produced by reacting (a) an alkoxylated amine of formula I with (b) phosphorous acid (H 3 PO 3 ).
- a boron compound of formula II, or one or more of the other boron compounds identified above is added to the reaction mixture of (a) and (b).
- the reaction of the boron compound is preferably substantially simultaneous with the reaction of the alkoxylated amine and the organic phosphite, as contrasted to the two step process disclosed for similar reaction products of U.S. Pat. No. 4,529,528. That is, all three reactants are added together prior to carrying out the reaction.
- reaction may also be carried out in a two step process in the manner of U.S. Pat. No. 4,529,528, either by first reacting the amine with the phosphorous acid and then reacting the resulting product with the boron compound, or first reacting the amine with the boron compound and then reacting the phosphorous acid with this product.
- two step reactions have been found to yield soluble, though not as preferred compounds.
- reaction of (a) the alkoxylated amine of Formula I and (b) phosphorous acid proceeds as follows when w of Formula I is 0: ##STR3##
- w of Formula I is 0: ##STR3##
- the reaction of (a) and (b) is carried out at a temperature of about 50° C. to about 250° C. and preferably, about 120° C. to about 180° C.
- (a) and (b) are reacted with (c) a boron compound selected from boric acid, a metaborate or a compound of the formula
- R 3 is a C 1 to C 6 alkyl group, and m and n are about 0 to 3, their sum being 3.
- the reaction of (a), (b) and (c) proceeds at a temperature such as noted above for the reaction of (a) and (b).
- the optimum reaction time varies with the amount of boron used.
- a monofunctional alcohol may be added to the reaction mixture in order to decrease the extent of polymerization in the final product.
- Appropriate monofunctional alcohols for use in the present invention are represented by formula III
- R 4 is a hydrocarbon group of 1 to 30 carbons.
- Preferred monofunctional alcohols are C 18 to C 26 alkyl chain length alcohols.
- a long-chain aliphatic carboxylic acid may be added to the reaction mixture in order to decrease the extent of polymerization in the reaction product.
- Appropriate long-chain aliphatic carboxylic acids are represented by formula IV ##STR5## wherein R 5 is a C 1 to C 30 hydrocarbon group.
- the long-chain aliphatic carboxylic acid represented by formula IV is oleic acid.
- the long-chain aliphatic carboxylic acid of formula IV may be first added to the alkoxylated amine and be allowed to react therewith.
- the long-chain aliphatic carboxylic acid will esterify one of the --OH groups on the amine.
- the phosphorous acid is added to this mixture with any necessary additional alkoxylated amine in order to react all of the phosphorous acid.
- reaction products are mixtures of a number of different simple and complex esters, including possibly cross-linked species and/or prepolymers.
- the organic oxides of the boron compounds may react with one or both of the alkoxy groups of the alkoxylated amines to yield water and/or organic alcohol by-products.
- the preferred mole ratio of the alkoxylated amine, phosphorous acid and the monofunctional alcohol or long-chain aliphatic carboxylic acid is 0.5:2 in any combination, and preferably 1:1:1.
- the optimum reaction time varies with the amount of boron being used, if any, but in general the reaction time should not exceed about 21/2 to 3 hours, and the long reaction times of U.S. Pat. No. 4,529,528 should be avoided.
- the water formed as a by-product may be removed by azeotropic distillation, and the cessation of the evolution of water generally marks the end of the reaction.
- 3 hours may be required, whereas for lesser amounts or no boron, 1.5 hours may be a sufficient reaction time.
- the present reaction is preferably carried out in the presence of a nitrogen blanket.
- the reaction may be carried out in the presence of a solvent, preferably a liquid hydrocarbon solvent such as toluene or xylene.
- a solvent preferably a liquid hydrocarbon solvent such as toluene or xylene.
- the solvent and any by-product alcohol may be removed, e.g., by vacuum stripping.
- reactions in which there is a low amount of boron compound generally need no solvent, due to the small amount of water evolved by the esterification reaction.
- a nitrogen blanket may be used to help sweep out some of the higher alcohol by-products, particularly where no solvent is used.
- the mix and nature of the reaction products will depend in part upon the proportion of the reactants contained in the reaction mixture. Molar ratios of alkoxylated amine to phosphorous acid in the range of about 0.1:1 to about 10:1 are believed to be satisfactory for the present invention, and ratios of about 0.5:1 to about 2:1 are preferred. Changing the relative amount of phosphorous acid compound in the reaction mixture in this manner tends to produce poorer results in the Falex EP test described below.
- the molar ratio of alkoxylated amine to boron compound is in the range of about 30:1 to about 1:1.
- the ratio of phosphorous acid to boron compound is suitably in the range of about 0.5:1 to about 20:1, and preferably about 1:1 to about 15:1.
- the use of low amounts of boron compound generally obviates the need for a solvent for carrying out the reaction, but the presence of higher amounts of boron compound in the above range provides generally superior results in various metalworking tests and operations.
- Alkoxylated amines which are useful in the present invention include, for example,
- Preferred alkoxylated amines for use in the present invention are di-lower hydroxyalkyl
- Preferred hydroxyalkyl groups are those in which R" is hydrogen or methyl or mixtures thereof.
- R is a C 1 to C 3 alkylene group. Examples include 2-hydroxyethyl and 2-hydroxypropyl.
- Alkoxylated amines of this series are commercially available, for example, from Armak Chemical Company under the trademarks ETHOMEEN, PROPOMEEN and PROPODUOMEEN.
- the boron compounds useful in the present invention include boric acid; mono-, di-and trimethyl borates; mono-, di- and tripropyl borates; mono-, di- and tributyl borates; mono-, di- and triamyl borates; mono-, di- and trihexyl borates; and silica borates.
- Boric acid is particularly preferred, primarily due to considerations of cost and availability.
- Useful monofunctional alcohols for use in the present invention are, e.g., Exxal 18 and Exxal 26, by Exxon Chemicals which are synthetic alcohols of C 18 and C 26 chain length.
- Sylfat 96 oleic acid from Sealand Chemicals may be preferably used as the long-chain aliphatic carboxylic acid in the present invention.
- Compounds of the present invention in the acid pH range are generally more effective in metalworking applications. Products in this pH range may suitably be achieved by raising the content of boron compound in the reaction mixture, as appropriate. On the other hand, the products should not be too highly acidic since this will result in corrosion of the metal being worked upon. In general, the compounds of the present invention are good rust inhibitors and do not require adjustment of acidity.
- a compound of the present invention has a pH of below about 5.5, it is desirable to adjust or pacify the pH to a range of about 5.5 to 7, and preferably 6 to 6.5, with an oil soluble amine.
- Suitable amines for adjustment of the pH include mixtures of long chain primary amines, which are commercially available from Rohm & Haas under the trademark PRIMENE 81R, or dimethyl decyl amine, which is commercially available from Ethyl Corporation under the trademark ADMA C 10 .
- Other pacifiers include commercially available rust inhibitors which are well known to the art.
- the compounds of the present invention are particularly useful as additives in various metalworking fluids to increase the lubricating capacity of the lubricating fluid and to reduce friction between metal parts.
- the compounds of the present invention will also have use in other lubricating environments, such as additives to engine and machinery lubricating oils.
- the compounds appear to be useful for the full range of metalworking fluids from mineral oils to synthetic oils to the so-called soluble oils, the latter being emulsifiable in water for more preferred aqueous metalworking environments which provide greater cooling capacity to the metalworking operation.
- the additives of the present invention are readily soluble in and compatible with any of these metalworking fluids.
- the compounds of the present invention may be used in conjunction with other metalworking fluid additives or formulation components, including sulfurized esters and active and passive sources of sulfur.
- Other additives including corrosion inhibitors, surface active agents, thickeners for forming greases, and additives for specialized formulation uses, may also be included.
- the compounds of the present invention are soluble in paraffinic or naphthenic base stocks up to at least about 10 weight percent, which is the practical limit for use.
- the compounds of the present invention are generally added in concentrations of about 0.1 to 10 weight percent, and typically about 1 to 6 weight percent.
- the compounds of the present invention are added in concentrations of about 0.1 to about 20 weight percent, and preferably about 0.25 to about 10 weight percent.
- the compounds of the present invention when added to metalworking fluids, provide a high degree of lubricity in any of a wide variety of metalworking or machining operations, including broaching, threading, tapping, reaming, gear cutting, deep drilling, milling, boring and various automatic screw machine operations.
- the additives of the present invention are particularly advantageous in extreme pressure (EP) operations.
- EP extreme pressure
- the compounds of the present invention When used to replace chlorinated paraffins or combinations of chlorinated paraffin with lard oil, the compounds of the present invention have been found to perform equally to or better than these conventional additives in a variety of lubricants, including drawing oils, tapping oils, gear oils and water-based metalworking formulations.
- Examples I-IX were tested in several standard tests which have been developed for metalworking fluids as described below.
- the compounds of the invention were compared to one or more of the following standard or competitive lubricants on the market: (1) LUBRIZOL LZ-5347, a PEP metalworking additive containing carbonated alkyl benzene sulfonates; and (2) a standard additive formulation comprising 25% P145 chlorinated wax (40% chlorine) from Dover Chemical Corp. and 75% lard oil.
- the 4-Ball Wear test (ASTM D-2266) measures the wear (displacement of metal by friction) when a test ball is rotated in a tetrahedral position on top of three stationary balls or discs. Wear is indicated by scar diameters on the three stationary balls or discs.
- each additive was dissolved at a concentration of 5% in Exxon 150N mineral oil or in the case of the emulsion was prepared as for the Texaco chip test above (5% modified oil in water or 0.75% additive in the total emulsion).
- the compounds of the present invention when added to mineral oil lubricants, show excellent metalworking properties as well as good corrosion resistance.
- the test results compare very favorably to reference oils such as chlorinated wax plus lard oil additive.
- the tests indicate an optimum concentration of about 3 weight percent when added to the lubricant oils.
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Abstract
Description
(R.sup.3 O).sub.m B(OH).sub.n (II)
R.sup.4 OH (III)
(R.sup.3 O).sub.m B(OH).sub.n (II)
R.sup.4 OH (III)
TABLE I ______________________________________ 4-BALL WEAR TEST (3% Additive in Exxon ISO 46 Oil) Additive Wear Scar (mm) ______________________________________ Example I 0.29 Example II 0.26 Example III 0.33 Example IV 0.39 Example V 0.37 Example VI 0.34 Example VII 0.33 Example VIII 0.42 Example IX 0.39 Lubrizol 5347 0.31 Chloroparaffin - Lard Oil 0.45 ______________________________________
TABLE II ______________________________________ EP TESTS 4-Ball EP Falex EP (3 wt. % (5 wt. % Additive) Additive) (in Exxon 150N) Torque (in Exxon 150N) Additive *Fail Load (lbs) at Fail LWI Weld ______________________________________ Example I 5,000+ 28-32 27.4 160 Example II 5,000+ 30-35 41.8 200 Example III 4,500+ 30-35 35.0 200 Example IV 4,600 30-35 34.7 200 Example V 4,800 30-35 36.0 200 Example VI >°5,500.sup. 30-35 41.8 200 Example VII 4,250 40-45 29.0 200 Example VIII 4,500+ 45 32.2 250 Example IX 6,500 30-35 39.6 200 Lubrizol 5347 .sup.x 4,100 .sup. 95 27.6 160 Chloroparaffin - 4,500+ 50 32.9 250 Lard Oil ______________________________________ *Values over 4,500 are `off scale` and are estimated values. °Pin would not fail (no break). .sup.x Excessive smoke and blackening of the pin and V blocks.
TABLE III ______________________________________ EP TESTS IN WATER BASED SYSTEMS (5% Additive in a Soluble Oil Base Diluted 19/1 with 100 ppm Water) Falex EP Torque 4-Ball EP Additive Fail Load, lbs. at Fail LWI Weld ______________________________________ Example I 4,000 50-55 26.6 126 Example II 4,000 45-50 21.2 100 Example III 4,050 45-50 21.4 100 Example IV 4,300 45-50 26.0 126 Example V 4,550 45-50 26.1 126 Example VI 4,600 45-50 31.1 126 Example VII 4,250 40-45 17.7 100 Example VIII 2,750 45 17.8 100 Example IX 3,750 50-55 25.0 100 Lubrizol 5347 4,050 70-75 29.6 126 Chloroparaffin - 3,750 55-60 25.7 100 Lard Oil ______________________________________
TABLE IV ______________________________________ RUST TESTS Cast Iron* Additive ASTM D-665A ASTM D-665B Chip Test ______________________________________ Example I Pass Fail Fail Example II Fail Fail Pass Example III Pass Fail Pass (near Pass) Example IV Pass Pass Fail Example V Fail Fail Fail (near Pass) Example VI Pass Pass Pass Example VII Pass Pass Pass Example VIII Pass Fail Fail Example IX Pass Pass Pass Lubrizol 5347 Pass Fail Fail Chloroparaffin - Fail Fail Fail Lard Oil ______________________________________ *5% additive in a soluble oil base, diluted 19/1 with water.
Claims (10)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/526,080 US5130036A (en) | 1990-05-18 | 1990-05-18 | Phosphorous amine lubricant additives |
EP90122031A EP0456888A1 (en) | 1990-05-18 | 1990-11-17 | Phosphorous amine lubricant additives |
JP3113075A JPH04227994A (en) | 1990-05-18 | 1991-05-17 | Phosphorous acic amine lubricant additive |
US07/911,839 US5194166A (en) | 1990-05-18 | 1992-07-10 | Phosphorous amine lubricant additives |
US08/013,510 US5348670A (en) | 1990-05-18 | 1993-02-04 | Phosphorous amine lubricant additives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/526,080 US5130036A (en) | 1990-05-18 | 1990-05-18 | Phosphorous amine lubricant additives |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/911,839 Division US5194166A (en) | 1990-05-18 | 1992-07-10 | Phosphorous amine lubricant additives |
Publications (1)
Publication Number | Publication Date |
---|---|
US5130036A true US5130036A (en) | 1992-07-14 |
Family
ID=24095831
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US07/526,080 Expired - Fee Related US5130036A (en) | 1990-05-18 | 1990-05-18 | Phosphorous amine lubricant additives |
US08/013,510 Expired - Fee Related US5348670A (en) | 1990-05-18 | 1993-02-04 | Phosphorous amine lubricant additives |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/013,510 Expired - Fee Related US5348670A (en) | 1990-05-18 | 1993-02-04 | Phosphorous amine lubricant additives |
Country Status (3)
Country | Link |
---|---|
US (2) | US5130036A (en) |
EP (1) | EP0456888A1 (en) |
JP (1) | JPH04227994A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5348670A (en) * | 1990-05-18 | 1994-09-20 | The Elco Corporation | Phosphorous amine lubricant additives |
US5362410A (en) * | 1993-09-13 | 1994-11-08 | Mobil Oil Corporation | Multifunctional ashless dispersants |
US5505868A (en) * | 1991-10-08 | 1996-04-09 | Ethyl Petroleum Additives Limited | Modified dispersant compositions |
US5612295A (en) * | 1994-05-18 | 1997-03-18 | Ethyl Corporation | Lubricant additive compositions |
CN115820329A (en) * | 2022-12-30 | 2023-03-21 | 太原理工大学 | Lubricating oil with layered boron phosphate amine compound as additive and preparation method thereof |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5817605A (en) * | 1991-06-03 | 1998-10-06 | Ethyl Petroleum Additives, Inc. | Automatic transmission and wet brake fluids and additive package therefor |
GB2285056B (en) * | 1991-06-03 | 1995-11-22 | Ethyl Petroleum Additives Inc | Automatic transmission and wet brake fluids and additive packages therefor |
US5346637A (en) * | 1992-12-16 | 1994-09-13 | Mobil Oil Corporation | Antiwear additives |
US5441656A (en) * | 1994-02-10 | 1995-08-15 | Ethyl Petroleum Additives, Inc. | Automatic transmission fluids and additives therefor |
US5891786A (en) * | 1995-01-12 | 1999-04-06 | Ethyl Corporation | Substantially metal free synthetic power transmission fluids having enhanced performance capabilities |
KR20000035819A (en) | 1996-08-30 | 2000-06-26 | 마크 에프. 웍터 | Novel water soluble metal working fluids |
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US3553131A (en) * | 1967-04-24 | 1971-01-05 | Mobil Oil Corp | Lubricant containing an aminephosphonate combined additive |
US4400284A (en) * | 1980-06-12 | 1983-08-23 | Union Oil Company Of California | Boron derivatives as lubricant additives |
US4427560A (en) * | 1981-12-10 | 1984-01-24 | Union Oil Company Of California | Anti-oxidation and corrosion inhibitors for boron-containing lubricants |
US4490265A (en) * | 1981-12-10 | 1984-12-25 | Union Oil Company Of California | Lubricating compositions |
US4522629A (en) * | 1983-09-23 | 1985-06-11 | Mobil Oil Corporation | Borated phosphonates as lubricant and fuel additives |
US4529528A (en) * | 1983-12-14 | 1985-07-16 | Mobil Oil Corporation | Borated amine-phosphite reaction product and lubricant and fuel containing same |
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US4533480A (en) * | 1983-03-18 | 1985-08-06 | Union Oil Company Of California | Bis(hydrocarbyloxy methylated) boron-containing, heterocyclic compounds and lubricating compositions containing the same |
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US5194166A (en) * | 1990-05-18 | 1993-03-16 | The Elco Corporation | Phosphorous amine lubricant additives |
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- 1990-11-17 EP EP90122031A patent/EP0456888A1/en not_active Ceased
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1991
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5348670A (en) * | 1990-05-18 | 1994-09-20 | The Elco Corporation | Phosphorous amine lubricant additives |
US5505868A (en) * | 1991-10-08 | 1996-04-09 | Ethyl Petroleum Additives Limited | Modified dispersant compositions |
US5362410A (en) * | 1993-09-13 | 1994-11-08 | Mobil Oil Corporation | Multifunctional ashless dispersants |
US5612295A (en) * | 1994-05-18 | 1997-03-18 | Ethyl Corporation | Lubricant additive compositions |
CN115820329A (en) * | 2022-12-30 | 2023-03-21 | 太原理工大学 | Lubricating oil with layered boron phosphate amine compound as additive and preparation method thereof |
CN115820329B (en) * | 2022-12-30 | 2023-10-31 | 太原理工大学 | Lubricant oil using layered boron phosphate amine compound as additive and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH04227994A (en) | 1992-08-18 |
EP0456888A1 (en) | 1991-11-21 |
US5348670A (en) | 1994-09-20 |
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